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Phenobarbital

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Phenobarbital FDA UDI
Generic Name
Phenobarbital therapeutic drug monitoring IVD, kit, fluorescent immunoassay FDA UDI
Model / Reference
20737860322 FDA UDI

Identifiers

Catalog Number
20737860322 FDA UDI
Primary DI / UDI-DI
04015630915774 FDA UDI
510(k) Number
K951595 FDA UDI
FDA Product Code
LGQ FDA UDI
GMDN Term
Phenobarbital therapeutic drug monitoring IVD, kit, fluorescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phenobarbital therapeutic drug monitoring IVD, kit, fluorescent immunoassay

Phenobarbital by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phenobarbital therapeutic drug monitoring IVD, kit, fluorescent immunoassay.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61c68307-edd4-42cb-abf1-793b75aaf720 35 fields · synced Jun 1, 2026